A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739962



Internal ID20515937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2158094..2158327hg38UCSC Ensembl
chr19:2158093..2158326hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739962
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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